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rs397508781

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508781(A;A)
Make rs397508781(A;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117535343
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508781
ebirs397508781
HLIrs397508781
Exacrs397508781
Varsomers397508781
Maprs397508781
PheGenIrs397508781
hapmaprs397508781
1000 genomesrs397508781
hgdprs397508781
ensemblrs397508781
gopubmedrs397508781
geneviewrs397508781
scholarrs397508781
googlers397508781
pharmgkbrs397508781
gwascentralrs397508781
openSNPrs397508781
23andMers397508781
23andMe allrs397508781
SNP Nexus

SNPshotrs397508781
SNPdbers397508781
MSV3drs397508781
GWAS Ctlgrs397508781
Max Magnitude0
ClinVar
Risk rs397508781(A;A)
Alt rs397508781(A;A)
Reference rs397508781(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117175397T>A
CLNSRC ClinVar
CLNACC RCV000047233.2,